As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies
Job Summary
As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.
ICON offers a range of benefits focused on well-being and work-life balance, including various annual leave entitlements, health insurance, retirement planning, and a global employee assistance program.
ICON is committed to fostering an inclusive and accessible environment, providing equal employment opportunities without discrimination and supporting reasonable accommodations for applicants.
Matching Summary
As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.
Skills & Requirements
Must-have
clinical trial monitoring
protocol compliance
data integrity management
patient safety assurance
site qualification and initiation
travel up to 60%
valid driver’s license
Nice-to-have
strong organizational skills
effective communication skills
ability to work independently
collaborative team player
attention to detail
fast-paced environment adaptability
Key Requirements
Bachelor's degree in scientific or healthcare field
Experience as a Clinical Research Associate
Knowledge of ICH-GCP guidelines
Ability to travel internationally and domestically